CAS 3303-31-9
:L-Leucyl-L-leucine
Description:
L-Leucyl-L-leucine, with the CAS number 3303-31-9, is a dipeptide composed of two leucine amino acids linked by a peptide bond. It is a member of the class of compounds known as peptides, which are formed by the condensation of amino acids. This dipeptide exhibits characteristics typical of hydrophobic amino acids due to the presence of leucine, which has a branched aliphatic side chain. As a result, L-Leucyl-L-leucine is generally insoluble in water but soluble in organic solvents. It plays a role in various biological processes, including protein synthesis and cellular signaling. The compound may also exhibit biological activity, influencing metabolic pathways and potentially serving as a building block for larger peptides or proteins. Its stability can be affected by factors such as pH and temperature, which are important considerations in both laboratory and biological contexts. Overall, L-Leucyl-L-leucine is significant in biochemistry and molecular biology, particularly in studies related to protein structure and function.
Formula:C12H24N2O3
InChI:InChI=1S/C12H24N2O3/c1-7(2)5-9(13)11(15)14-10(12(16)17)6-8(3)4/h7-10H,5-6,13H2,1-4H3,(H,14,15)(H,16,17)/t9-,10-/m0/s1
InChI key:InChIKey=LCPYQJIKPJDLLB-UWVGGRQHSA-N
SMILES:[C@H](NC([C@H](CC(C)C)N)=O)(CC(C)C)C(O)=O
Synonyms:- 10: PN: WO2020097235 SEQID: 239 claimed protein
- 11: PN: US20090239809 SEQID: 11 claimed protein
- 2: PN: CN101845080 PAGE: 2 claimed protein
- 38: PN: EP2161028 PAGE: 10 claimed protein
- 456: PN: EP2071334 SEQID: 488 claimed protein
- 456: PN: WO2009077864 SEQID: 488 claimed protein
- <span class="text-smallcaps">L</smallcap>-Leucine, <smallcap>L</span>-leucyl-
- <span class="text-smallcaps">L</smallcap>-Leucine, N-<smallcap>L</span>-leucyl-
- <span class="text-smallcaps">L</smallcap>-Leucinyl-<smallcap>L</span>-leucine
- <span class="text-smallcaps">L</smallcap>-Leucyl-<smallcap>L</span>-leucine
- H-Leu-Leu-OH
- L-Leucyl-L-leucine
- Leucine, N-<span class="text-smallcaps">L</smallcap>-leucyl-, <smallcap>L</span>-
- Leucine, N-<span class="text-smallcaps">L</span>-leucyl-
- Leucylleucine
- NSC 89185
- Leucine, N-L-leucyl-, L-
- Leucine, N-L-leucyl-
- L-Leucine, N-L-leucyl-
- See more synonyms
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Found 8 products.
H-Leu-Leu-OH
CAS:Dileucine, substrate for dipeptidase activity measurement in serum and tissues as well as urine. LL forms nanotubes.Formula:C12H24N2O3Purity:> 99%Color and Shape:White PowderMolecular weight:244.33(S)-2-((S)-2-Amino-4-Methylpentanamido)-4-Methylpentanoic Acid
CAS:<p>(S)-2-((S)-2-Amino-4-Methylpentanamido)-4-Methylpentanoic Acid</p>Purity:98%Molecular weight:244.33g/molLeu-Leu-OH
CAS:<p>Leu-Leu-OH is a derivative dipeptide of leucine that can be used to study the function of the double leucine motif, is present as a metabolite.</p>Formula:C12H24N2O3Purity:99.34%Color and Shape:SolidMolecular weight:244.33(S)-2-((S)-2-Amino-4-methylpentanamido)-4-methylpentanoic Acid
CAS:<p>Applications (S)-2-((S)-2-Amino-4-methylpentanamido)-4-methylpentanoic acid (cas# 3303-31-9) is a useful research chemical.<br></p>Formula:C12H24N2O3Color and Shape:NeatMolecular weight:244.33Leu-Leu-OH
CAS:<p>Leu-Leu-OH is a polymerase chain that belongs to the group of p2. It has been used as an experimental model for biological studies and cell lysis. The activity of Leu-Leu-OH is due to hydrogen bonding interactions with water molecules. This polymerase chain has been shown to be involved in infectious diseases, autoimmune diseases, and toll-like receptor signaling pathways. Leu-Leu-OH has also been studied as a model system for apoptosis by cell factor and histological analysis in anhydrous sodium phosphate buffer at pH 7.4.</p>Formula:C12H24N2O3Purity:Min. 95%Color and Shape:PowderMolecular weight:244.33 g/mol








